Garner R C, Pickering C, Martin C N
Chem Biol Interact. 1979 Jul;26(2):197-205. doi: 10.1016/0009-2797(79)90023-1.
Methyl- (MNUA), ethyl- (ENUA), propyl- (PNUA) and butylnitrosourea (BNUA) have been tested for toxicity and mutation in a liquid suspension assay towards Escherichia coli WP2 and some of its repair deficient derivatives. A comparison of survival rates after nitrosourea exposure between WP2 and WP2 uvrA showed no difference between the two strains but a consistent difference in potency between the various nitrosoureas studied. Toxicity increased in the order MNUA less than PNUA less than ENUA less than BNUA. ENUA and PNUA induced a greater number of trp+ revertants in both strains than did MNUA and BNUA, particularly at low survival rates. None of these differences in biological potency could be accounted for by differences in rates of hydrolysis. ENUA, PNUA and BNUA were non-mutagenic towards WP2 lexA, WP2 recA and WP2 uvrA lexA, whereas MNUA did induce mutations. Ethyl methanesulphonate (EMS) was able to mutate WP2 lexA. These results are discussed in the light of current theories regarding the mechanism of action of these compounds.
已在液体悬浮试验中对甲基亚硝基脲(MNUA)、乙基亚硝基脲(ENUA)、丙基亚硝基脲(PNUA)和丁基亚硝基脲(BNUA)针对大肠杆菌WP2及其一些修复缺陷衍生物的毒性和致突变性进行了测试。WP2和WP2 uvrA在亚硝基脲暴露后的存活率比较显示,这两种菌株之间没有差异,但在所研究的各种亚硝基脲之间效力存在一致差异。毒性按MNUA<PNUA<ENUA<BNUA的顺序增加。与MNUA和BNUA相比,ENUA和PNUA在两种菌株中诱导出更多的trp+回复突变体,尤其是在低存活率时。这些生物学效力的差异均不能用水解速率的差异来解释。ENUA、PNUA和BNUA对WP2 lexA、WP2 recA和WP2 uvrA lexA无致突变性,而MNUA确实会诱导突变。甲磺酸乙酯(EMS)能够使WP2 lexA发生突变。根据关于这些化合物作用机制的当前理论对这些结果进行了讨论。